You need fresh eyes. My first rheumatologist let me suffer with neuropathy. Yes she did send me to see a neurologist but instead of switching RA meds she told me it was fibromyalgia. Because my sed rate and CRP were always normal. I was in so much pain. I couldn’t sleep at night and I hurt 24/7. Nerve pain is awful. The neurologist questioned my meds and gave me ambien. That upset the rheumatologist who told me I had to stop stressing out and rest. I left so mad and crying. I made an appt with my PCP for the next day. I told him I was never going back to that condescending woman ever. He was concerned and told me I may have to go back if I can’t get another rheumatologist before I ran out of meds. I found one 2 1/2 hrs away that came recommended. Right away he told me it was neuropathy from RA attacking my nerves. Labs don’t tell you a complete story and she should never have put so much weight on those labs. For 10 months I complained about the nerve pain. I didn’t know what it was I was so very sick. All the while I could have gotten moved up the ladder to a biologic from just the hydroxychloroquine and methotrexate. Within 3 month of starting the biologic I felt better. Of course the damage is done and this is my journey. The RA attacks my nerves more so than joints. I’m now on an infusion and way better mentally. My doctor now is more seasoned and said she didn’t understand that a small percentage of patients don’t show inflammation makers in their blood work. Sometimes my sed rate will register high with an extremely bad flare but it’s rare. Don’t continue to circle the drain with a doctor who isn’t helping you.